These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 1646293)

  • 1. Wocko, a neurological mutant generated in a transgenic mouse pedigree.
    Crenshaw EB; Ryan A; Dillon SR; Kalla K; Rosenfeld MG
    J Neurosci; 1991 Jun; 11(6):1524-30. PubMed ID: 1646293
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Altered circadian rhythmicity in the Wocko mouse, a hyperactive transgenic mutant.
    Sollars PJ; Ryan A; Ogilvie MD; Pickard GE
    Neuroreport; 1996 May; 7(7):1245-8. PubMed ID: 8817541
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A transgenic insertional inner ear mutation on mouse chromosome 1.
    Friedman RA; Adir Y; Crenshaw EB; Ryan AF; Rosenfeld MG
    Laryngoscope; 2000 Apr; 110(4):489-96. PubMed ID: 10763993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid genotyping of mutant mice using dried blood spots for polymerase chain reaction (PCR) analysis.
    Campbell DB; Hess EJ
    Brain Res Brain Res Protoc; 1997 May; 1(2):117-23. PubMed ID: 9385073
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation.
    Pau H; Hawker K; Fuchs H; De Angelis MH; Steel KP
    Otol Neurotol; 2004 Sep; 25(5):707-13. PubMed ID: 15353999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Insertional mutagenesis inducing hypomyelination in transgenic mice.
    Orian JM; Mitchell AW; Marshman WE; Webb GC; Ayers MM; Grail D; Ford JH; Kaye AH; Gonzales MF
    J Neurosci Res; 1994 Dec; 39(5):604-12. PubMed ID: 7534359
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.
    Alagramam KN; Kwon HY; Cacheiro NL; Stubbs L; Wright CG; Erway LC; Woychik RP
    Genetics; 1999 Aug; 152(4):1691-9. PubMed ID: 10430593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.
    Ting CN; Kohrman D; Burgess DL; Boyle A; Altschuler RA; Gholizadeh G; Samuelson LC; Jang W; Meisler MH
    Genetics; 1994 Jan; 136(1):247-54. PubMed ID: 7511123
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer.
    Alagramam KN; Zahorsky-Reeves J; Wright CG; Pawlowski KS; Erway LC; Stubbs L; Woychik RP
    Hear Res; 2000 Oct; 148(1-2):181-91. PubMed ID: 10978835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.
    Alagramam KN; Murcia CL; Kwon HY; Pawlowski KS; Wright CG; Woychik RP
    Nat Genet; 2001 Jan; 27(1):99-102. PubMed ID: 11138007
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 221-bp fragment of the mouse opsin promoter directs expression specifically to the rod photoreceptors of transgenic mice.
    Quiambao AB; Peachey NS; Mangini NJ; Röhlich P; Hollyfield JG; al-Ubaidi MR
    Vis Neurosci; 1997; 14(4):617-25. PubMed ID: 9278991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lim2(To3) transgenic mice establish a causative relationship between the mutation identified in the lim2 gene and cataractogenesis in the To3 mouse mutant.
    Steele EC; Wang JH; Lo WK; Saperstein DA; Li X; Church RL
    Mol Vis; 2000 Jun; 6():85-94. PubMed ID: 10851259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ontogeny of hyperactivity and circling behavior in a transgenic insertional mutant mouse.
    Fitzgerald LW; Ratty AK; Miller KJ; Ellsworth MK; Glick SD; Gross KW
    Behav Neurosci; 1991 Oct; 105(5):755-63. PubMed ID: 1815622
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of an allele of reeler by insertional mutagenesis.
    Miao GG; Smeyne RJ; D'Arcangelo G; Copeland NG; Jenkins NA; Morgan JI; Curran T
    Proc Natl Acad Sci U S A; 1994 Nov; 91(23):11050-4. PubMed ID: 7972007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice.
    Sarsero JP; Li L; Holloway TP; Voullaire L; Gazeas S; Fowler KJ; Kirby DM; Thorburn DR; Galle A; Cheema S; Koenig M; Williamson R; Ioannou PA
    Mamm Genome; 2004 May; 15(5):370-82. PubMed ID: 15170226
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse.
    Mochizuki E; Okumura K; Ishikawa M; Yoshimoto S; Yamaguchi J; Seki Y; Wada K; Yokohama M; Ushiki T; Tokano H; Ishii R; Shitara H; Taya C; Kitamura K; Yonekawa H; Kikkawa Y
    Exp Anim; 2010; 59(1):57-71. PubMed ID: 20224170
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Developmental regulation of the membrane properties of central vestibular neurons by sensory vestibular information in the mouse.
    Eugène D; Deforges S; Guimont F; Idoux E; Vidal PP; Moore LE; Vibert N
    J Physiol; 2007 Sep; 583(Pt 3):923-43. PubMed ID: 17627998
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive neuromuscular disorder in a transgenic line of mice.
    Kelly D; Chancellor K; Milatovich A; Francke U; Suzuki K; Popko B
    J Neurosci; 1994 Jan; 14(1):198-207. PubMed ID: 7506762
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Symplastic spermatids (sys): a recessive insertional mutation in mice causing a defect in spermatogenesis.
    MacGregor GR; Russell LD; Van Beek ME; Hanten GR; Kovac MJ; Kozak CA; Meistrich ML; Overbeek PA
    Proc Natl Acad Sci U S A; 1990 Jul; 87(13):5016-20. PubMed ID: 2164218
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation.
    Mjaatvedt CH; Yamamura H; Capehart AA; Turner D; Markwald RR
    Dev Biol; 1998 Oct; 202(1):56-66. PubMed ID: 9758703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.